Association between chemokine receptor 3T51C gene polymorphism and different clinical asthma phenotypes in Egyptian asthmatic children

IF 0.2 Q4 RESPIRATORY SYSTEM
M. Zedan, Mona El wassefy, I. Nour, E. Khashaba, A. Osman, E. El Sherbiny
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引用次数: 1

Abstract

Background Asthma is a heterogeneous disorder, which is affected by interaction between genes and the surrounding environment. Chemokine receptor 3 (CCR3) which is expressed over eosinophils and Th2 lymphocytes has a significant role in chemoattraction of those cells to inflammatory sites which symbolizes a key mechanism in asthma. Aim A trial to detect the association between CCR3 T51C gene polymorphism and different asthma phenotypes (allergic march phenotype, cough-predominant asthma phenotype, and wheeze-predominant asthma phenotype). Patients and methods A case–control study was conducted comprising 60 asthmatic patients and 100 healthy controls. Asthmatic children were divided into three groups of 20 patients each, group 1 allergic march phenotype (wheeze asthma phenotype with allergic rhinitis and/or atopic dermatitis), group 2 cough-predominant asthma phenotype, and group 3 wheeze-predominant asthma phenotype. The included cases and controls underwent total serum immunoglobulin E (IgE) using the enzyme-linked immunosorbent assay technique, peripheral eosinophilic percent, and PCR-restriction fragment length polymorphism for CCR3 T51C gene polymorphism. Results Asthmatic children showed significant increase in crowding index, family history of bronchial asthma, parental smoking, parental consanguinity, and total serum IgE than controls. Also, the CCR3 T51C gene polymorphism was found in Egyptian asthmatic children but no significant association concerning this polymorphism and different clinical asthma phenotypes was detected. Conclusion In conclusion, allergic march phenotype showed significant higher frequency with positive family history of asthma when compared with cough and wheezy asthma phenotypes. Also, parental consanguinity showed higher frequency in cough phenotype compared with allergic march phenotype. Furthermore, the CCR3 T51C gene polymorphism is found to be present in Egyptian asthmatic children, but there is no significant association between CCR3 T51C gene polymorphism and different asthma phenotypes. So, larger scale studies are needed. However, the TT genotype showed higher frequency in the studied phenotypes compared with CC and CT genotypes while asthmatic cases with the CC genotype showed higher total serum IgE compared with those with TT and CT genotypes.
趋化因子受体3T51C基因多态性与埃及哮喘患儿不同临床哮喘表型的关系
哮喘是一种异质性疾病,受基因和周围环境相互作用的影响。趋化因子受体3 (CCR3)在嗜酸性粒细胞和Th2淋巴细胞上表达,在这些细胞向炎症部位的化学吸引中起着重要作用,这是哮喘的关键机制。目的探讨CCR3 T51C基因多态性与哮喘不同表型(变应性哮喘表型、咳嗽型哮喘表型和喘息型哮喘表型)的相关性。患者与方法采用60例哮喘患者和100例健康对照进行病例-对照研究。将哮喘患儿分为3组,每组20例,1组为变应性进行表型(喘息型哮喘伴变应性鼻炎和/或特应性皮炎),2组为咳嗽型哮喘,3组为喘息型哮喘。采用酶联免疫吸附测定技术检测血清总免疫球蛋白E (IgE)、外周血嗜酸性粒细胞百分比、pcr -限制性片段长度多态性检测CCR3 T51C基因多态性。结果哮喘患儿的拥挤指数、支气管哮喘家族史、父母吸烟、父母亲缘关系、血清总IgE均明显高于对照组。此外,CCR3 T51C基因多态性在埃及哮喘儿童中发现,但该多态性与不同临床哮喘表型无显著相关性。结论哮喘家族史阳性的变应性行军表型明显高于咳嗽和喘息型表型。与变应性三月型相比,亲本亲属型在咳嗽表型中出现的频率更高。此外,在埃及哮喘儿童中发现CCR3 T51C基因多态性存在,但CCR3 T51C基因多态性与不同哮喘表型之间无显著相关性。因此,需要更大规模的研究。然而,TT基因型在研究表型中的频率高于CC和CT基因型,而CC基因型哮喘患者的血清总IgE高于TT和CT基因型。
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来源期刊
自引率
0.00%
发文量
46
审稿时长
22 weeks
期刊介绍: The journal will cover technical and clinical studies related to health, ethical and social issues in field of The Egyptian Journal of Chest Diseases and Tuberculosis aims to publish and inform readers and all chest physicians of the progress in medical research concerning all aspect of chest diseases. Publications include original articles review articles, editorials, case studies and reports which are relevant to chest diseases. The Journal also aims to highlight recent updates in chest medicine. . Articles with clinical interest and implications will be given preference.
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